
CAS 31754-00-4
:3-(3-CARBOXYPROPIONYLAMINO)PHENYLBORONIC ACID
Description:
3-(3-Carboxypropionylamino)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with an amino group and a carboxypropionyl group, contributing to its potential applications in medicinal chemistry and biochemistry. The carboxylic acid moiety enhances its solubility in polar solvents and may participate in various chemical reactions, including esterification and amidation. The boronic acid functionality allows for interactions with biomolecules, making it useful in drug development and as a tool in chemical biology for targeting specific cellular pathways. Additionally, the compound's structure suggests potential for use in materials science, particularly in the development of sensors or catalysts. Overall, 3-(3-Carboxypropionylamino)phenylboronic acid is a versatile compound with significant implications in both research and practical applications.
Formula:C10H12BNO5
Synonyms:- Butanoic acid, 4-[(3-boronophenyl)amino]-4-oxo-
- N-(3-PHENYLBORONIC)SUCCINAMIC ACID
- 4-(3-boronoanilino)-4-oxobutanoic acid
- 3-(3-CARBOXYPROPIONYLAMINO)PHENYLBORONIC ACID
- N-[3-(Dihydroxyboryl)phenyl]succinamidic acid
- 4-((3-Boronophenyl)amino)-4-oxobutanoic acid
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Found 3 products.
3-(3-Carboxypropionylamino)phenylboronic acid
CAS:Formula:C10H12BNO5Purity:98%Color and Shape:SolidMolecular weight:237.01703-(3-Carboxypropionylamino)phenylboronic acid
CAS:3-(3-Carboxypropionylamino)phenylboronic acidPurity:≥95%Molecular weight:237.02g/mol3-(3-Carboxypropionylamino)phenylboronic acid
CAS:Formula:C10H12BNO5Purity:95.0%Color and Shape:SolidMolecular weight:237.02


